Drug Guide

Generic Name

Methoxyflurane

Brand Names Penthrane

Classification

Therapeutic: Anesthetic, Sedative

Pharmacological: Inhalational anesthetic agent

FDA Approved Indications

  • Use as an inhalational anesthetic for induction and maintenance of anesthesia.

Mechanism of Action

Methoxyflurane produces anesthesia by enhancing the activity of GABA_A receptors in the central nervous system, leading to increased chloride conductance and neuronal hyperpolarization.

Dosage and Administration

Adult: Administer via inhalation using approved equipment; dose depends on procedure and patient response.

Pediatric: Use not approved officially; consult specialized guidelines.

Geriatric: Careful titration required due to increased sensitivity; monitor closely.

Renal Impairment: Use with caution; may accumulate and cause toxicity.

Hepatic Impairment: Use cautiously; liver function may influence metabolism.

Pharmacokinetics

Absorption: Readily absorbed via inhalation.

Distribution: Widely distributed throughout the body, crossing the blood-brain barrier.

Metabolism: Minimal metabolism; mainly exhaled unchanged.

Excretion: Primarily exhaled unchanged through the lungs.

Half Life: Approximately 2-3 minutes in healthy individuals.

Contraindications

  • Known hypersensitivity to methoxyflurane or other halogenated anesthetics.
  • History of malignant hyperthermia.

Precautions

  • Use with caution in patients with renal or hepatic impairment, cardiac disease, or increased intracranial pressure.

Adverse Reactions - Common

  • Dizziness (Frequent)
  • Nausea (Frequent)
  • Headache (Common)
  • Fatigue (Common)

Adverse Reactions - Serious

  • Malignant hyperthermia (Rare)
  • Hepatotoxicity (Rare)
  • Malignant hyperthermia (Rare)
  • Cardiac arrhythmias (Rare)

Drug-Drug Interactions

  • Concurrent use with other halogenated anesthetics or medications that sensitize the myocardium to arrhythmias.

Drug-Food Interactions

N/A

Drug-Herb Interactions

N/A

Nursing Implications

Assessment: Monitor vital signs, oxygen saturation, and neurological status.

Diagnoses:

  • Risk for impaired gas exchange.
  • Risk for impaired neurological function.

Implementation: Administer under supervision in a facility equipped for anesthesia; monitor closely.

Evaluation: Ensure effective anesthesia with minimal adverse effects; monitor recovery and any adverse reactions.

Patient/Family Teaching

  • Instruct about the purpose of the inhalation agent.
  • Warn about possible dizziness, nausea, and coordination impairment.
  • Advise to report any unusual symptoms immediately.

Special Considerations

Black Box Warnings:

  • Potential for hepatotoxicity; use with caution, especially in long-term or repeated applications.

Genetic Factors: N/A

Lab Test Interference: May interfere with liver function tests if hepatotoxicity occurs.

Overdose Management

Signs/Symptoms: Hypotension, bradycardia, anesthesia overdose, hepatotoxicity.

Treatment: Discontinue administration immediately; supportive care; monitor vital signs; provide oxygen and ventilation support as needed.

Storage and Handling

Storage: Store in a cool, dry place away from heat and ignition sources.

Stability: Stable under recommended storage conditions.

This guide is for educational purposes only and is not intended for clinical use.